ZIMMER Dermatome AN - Indonesia BPOM Medical Device Registration
ZIMMER Dermatome AN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022384. The device is manufactured by ZIMMER SURGICAL., INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZIMMER SURGICAL., INCCountry of Origin
United States
Authorized Representative
PT. KALMED SEJAHTERA INDONESIAAR Address
Jl. TMII Pintu II No. 2, RT 006 RW 004,
Registration Date
Apr 26, 2020
Expiry Date
Nov 11, 2024
Product Type
Surgical Equipment
Surgical instrument motors and accessories/attachments.
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